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The outcome of radiation therapy as a primary treatment in orbital lymphoma: a systematic review

Thalia Puteri Oktariana1, Aisha Andriana1, Rafiq Sulistyo Nugroho2
Rep Pract Oncol Radiother 2022;27(4):724-733.

Abstract

Background: The extranodal marginal-zone B-cell lymphomas of mucosa-associated lymphoid tissue (MALT) is the most common orbital and adnexal lymphomas. Radiotherapy is one of the most preferred treatment options for orbital lymphomas since they are localized and radiation sensitive. The objective of this study is to evaluate how radiation therapy affected the outcome of orbital MALT lymphoma.

Materials and ethods: PRISMA guideline was used to conduct this systematic review of electronic databases (PubMed, EMBASE and Cochrane Library), then we assessed the quality of evidence of each paper.

Results: Twenty-five studies were finally included. 94% studies were intended for definitive therapy and almost all of the studies used external radiation sources. The total doses given to the tumor bed ranged from 4 Gy to 55 Gy and were divided into three groups: ultra-low dose (4–6 Gy), standard-dose (24–30.6 Gy), and high-dose (> 30.6 Gy). 75-90% patients showed CR and local relapse was only reported at 3.5–5%. Higher 5-year PFS was reported in the patients group with lens shielding (90.1% vs. 82.1%) and an increase in Meiboscore after RT courses. Toxicities, including dry eye and cataract, were reported in several patients. Acute toxicities subsided gradually over a few months with artificial tears. The risk of early cataract formation increases in patients who received > 30 Gy and lower in the IMRT group.

Conclusion: RT is a successful primary definitive therapy for low-grade orbital MALT lymphoma, with a high survival rate, low recurrence rate, and typically acceptable toxicity.

review article

Reports of Practical Oncology and Radiotherapy

2022, Volume 27, Number 4, pages: 724–733

DOI: 10.5603/RPOR.a2022.0065

Submitted: 30.01.2022

Accepted: 06.05.2022

© 2022 Greater Poland Cancer Centre.

Published by Via Medica.

All rights reserved.

e-ISSN 2083–4640

ISSN 1507–1367

The outcome of radiation therapy as a primary treatment in orbital lymphoma: a systematic review

Thalia Puteri Oktariana1Aisha Andriana1Rafiq Sulistyo Nugroho2
1Faculty of Medicine, Universitas Brawijaya, Malang, East Java, Indonesia
2Department of Radiotherapy, Saiful Anwar General Hospital, Malang, East Java, Indonesia

Address for correspondence: Thalia Puteri Oktariana, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia, Jl. Veteran No. 1, Lowokwaru, Malang; e-mail: thalia.oktariana@gmail.com

This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially

Abstract
Background: The extranodal marginal-zone B-cell lymphomas of mucosa-associated lymphoid tissue (MALT) is the most common orbital and adnexal lymphomas. Radiotherapy is one of the most preferred treatment options for orbital lymphomas since they are localized and radiation sensitive. The objective of this study is to evaluate how radiation therapy affected the outcome of orbital MALT lymphoma.
Materials and methods: PRISMA guideline was used to conduct this systematic review of electronic databases (PubMed, EMBASE and Cochrane Library), then we assessed the quality of evidence of each paper.
Results: Twenty-five studies were finally included. 94% studies were intended for definitive therapy and almost all of the studies used external radiation sources. The total doses given to the tumor bed ranged from 4 Gy to 55 Gy and were divided into three groups: ultra-low dose (4–6 Gy), standard-dose (24–30.6 Gy), and high-dose (> 30.6 Gy). 75–90% patients showed CR and local relapse was only reported at 3.5–5%. Higher 5-year PFS was reported in the patients group with lens shielding (90.1% vs. 82.1%) and an increase in Meiboscore after RT courses. Toxicities, including dry eye and cataract, were reported in several patients. Acute toxicities subsided gradually over a few months with artificial tears. The risk of early cataract formation increases in patients who received > 30 Gy and lower in the IMRT group.
Conclusion: RT is a successful primary definitive therapy for low-grade orbital MALT lymphoma, with a high survival rate, low recurrence rate, and typically acceptable toxicity.
Key words: radiation therapy; radiotherapy; orbital tumor; MALT; lymphoma
Rep Pract Oncol Radiother 2022;27(4):724–733

Introduction

Non-lymphoma Hodgkin’s was found in about 55% of primary orbital malignancies in adults. Extranodal marginal zone B-cell lymphomas of mucosa-associated lymphoid tissue (MALT) type account for the majority of non-lymphomas Hodgkin’s of the orbit and adnexa. The conjunctiva, eyelid, lacrimal gland, and retrobulbar region are commonly affected by orbital MALT lymphomas (OAML). It is characterized by an indolent course and a confined tumor that is predominantly radiation sensitive [1–3].

As an initial treatment for orbital MALT lymphoma, radiation therapy (RT) was known to be beneficial. For localized disease, radiotherapy has often been the treatment of choice. Compared to surgery, it provides superior local control and cure. Low to moderate radiation doses (25–36 Gy) are thought to be capable of achieving 95–100% local control. However, the ideal radiation dose for the treatment of orbital adnexal lymphoma that achieves a high local control rate with a low risk of visually noticeable sequelae is unknown. So, a variety of approaches, involving radiation dose, volume, and lens shielding, have been used [1–4].

Therefore, we conducted a systematic review to see how successful different doses and procedures of radiation therapy were for treating orbital MALT lymphoma.

Materials and methods

We conducted a systematic review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) statement. We searched the terms “Ocular Lymphoma”, “Orbital Lymphoma”, “MALT”, “Radiotherapy”, “Radiation therapy”, and “IMRT” with time restriction from 2012 to 2022 in various electronic databases such as PubMed, EMBASE and Cochrane Library. The focus of the search was the outcome of the radiotherapy on the clinical application to the orbital lymphoma. We included full-text publications reporting orbital lymphoma at different ages. Literature which focused on orbital lymphoma that had been treated with radiotherapy, the doses of the radiotherapy used for treatment of orbital lymphoma, and also the response of radiation therapy to orbital lymphoma were searched and included. We considered only human-based topics and articles published in English. No full-text publications, duplicates, letters to editor, and articles with no radiotherapy effect on orbital lymphoma were excluded.

Two researchers evaluated the studies independently to determine the final articles to be included, and the final decision was reached by consensus with another author. All evidence was assessed by the Newcastle-Ottawa Scale (NOS) for cohort studies. The study is classified as high quality if it gets 3 or 4 points in the selection domain AND 1 or 2 points in the comparability domain AND 2 or 3 points in the outcome domain [5]. The Joanna Briggs Institute (JBI) scale was used to evaluate the risk of bias from included case reports. It assessed demographic characteristics, past medical history, current condition, diagnostic assessment, treatment procedure, post-intervention condition, adverse events, and lessons to learn. The total score was categorized as low (0–3) and high quality (4–8) [6].

154914.png
Figure 1. Flow diagram of study selection process

Results

Eligible studies

A total of 329 articles were identified through PUBMED, EMBASE, and Cochrane library. Eighty seven studies were removed because of duplication. The first selection was performed based on the title and abstract of the articles. We excluded 210 articles that did not meet the inclusion criteria. In further screening, 7 articles were omitted because of the lack of data. So, 25 studies were finally included in this systematic review.

Baseline characteristics

All included articles have a high score. The mean score of the NOS for the cohort studies was 7.4. The mean score of case reports in the JBI scale was 7.1. These results support that the 25 included studies were high quality on average. Baseline characteristics of the included studies are summarized in Table 1.

Table 1. Baseline characteristics

No

Study

Primary cancer sites

Purpose

RT method

Doses

Responses

Toxicities

Retrospective Cohort

1

Xu et al., 2021

Orbital and ocular adnexal MALT

Definitive

EBRT (IMRT) + electron beam with or without lens-sparing method

A: 20 Gy/10 Fr EBRT+ 14 Gy/7 Fr Electron beam using lens shield

B: 32 Gy/16 Fr or 34 Gy/17 Fr without lens shield

5-year & 10-year OS: 100%

5-year DFS: 96.7%

10-year DFS: 74.2%

No local recurrence developed

3 patients developed distant metastasis

Acute: periorbital soft tissue swelling, dry eye, conjunctivitis

Late: Patients aged60 years had a 4.43-times higher risk of cataract incidence

The median cataract incidence period was longer in the lens shielding group

2

Lee et al., 2021

Early-stage ocular adnexal MALT

Definitive

Electron beam with lens shielding

4 Gy in two fractions over 2 days

75% achieved CR

25% achieved PR

No adverse events reported

3

Leeson et al., 2021

Early stage ocular adnexal MALT

Definitive

EBRT (3D-CRT or VMAT)

2030 Gy with 1.52 Gy fraction sizes

Excellent local disease control & no local recurrence

Acute : one patient experienced tearing and red eye

Late : one patient experienced dry eye and cataract formation

Both occurred in the same patient, who received 26Gy to the orbit using 3D-CRT

4

Rehn et al., 2020

Indolent ocular adnexal lymphoma

Definitive

EBRT (IMRT)

EBRT (Conventional)

450.4 Gy in 0.52 Gy fraction sizes.

High-dose RT: 29 patients

Standard-dose RT: 17 patients

Ultra-low-dose RT: 6 patients

Overall response rate : 94%

High-dose CR: 90%

Standard-dose CR: 82%

Ultra-low-dose CR: 50%

10-year local control : 100%

Acute : conjunctivitis, dry eye, & tearing

Late : dry eye, cataract

Lower frequencies of adverse effect in IMRT group

5

Niwa et al., 2020

Ocular adnexal MALT

Definitive

EBRT

3036 Gy in 1518 fractions

69.1% had a CR

18.5% had a PR

3.7% had a stable disease

Acute : no acute morbidities

Late : dry eye (3.7%), punctate keratitis(4.9%), cataract (2.5%)

6

Kim et al., 2020

Orbital lymphoma

Definitive

EBRT (IMRT)

EBRT (3D-CRT)

Electron beam

Orbital-type: 30.6-36 Gy in 1720 fractions

Conjunctival: 23.425.2 Gy in 1314 fractions

Increase in meiboscore

No patient had development of severe dry eye with corneal erosion or vision compromise

7

Jeon et al., 2018

Ocular adnexal MALT

Definitive

EBRT

2432 Gy in 1.82 Gy fraction sizes

92% achieved complete response

Acute: dry eye

Late: dry eye (58%), cataract(22%)

8

Pinnix et al., 2017

Ocular adnexal lymphoma

Definitive

EBRT

4 Gy in 2 fractions over 2 days

86.4% patients had a CR and 13.6% patients had a PR

Acute: dry eye (4.5%)

Late: no adverse effect reported

9

Li, 2018

Ocular adnexal MALT

Definitive

EBRT

Total dose ranged 30-55 Gy, mostly 34 Gy/17 fractions

Complete response and no progression

Dry eye syndrome (9%), cataract (4.5%), vision loss (4.5%)

10

Platt, 2017

Ocular adnexal EMZL

Definitive

EBRT (3D-CRT, electron beam, & IMRT)

2036 Gy in 1.52 Gy fraction sizes

No recurrence in the irradiation field.

86.66% visual acuity improvement.

Acute : no adverse event reported

Late : cataract (31.6%), retinopathy (1.7%), retinal detachment (3.3%)

11

Park et al., 2017

Ocular adnexal MALT

Definitive

EBRT(single anterior field, 3D-CRT, IMRT)

Electron beams with lens shield

Electron beams with hanging block

2245 Gy in 1.82 Gy fraction sizes

100% complete response

88.1% overall progression free survival

90.1% 5-year PFS in patients with lens protection

82.1% 5-year PFS in patients without lens protection

Acute: periorbital dermatitis (26.8%)

Late: xerophthalmia (43.3%), cataract (11.9%), ptosis (4.5%), lacrimal duct obstruction (1.5%)

12

Shirota et al., 2017

Ocular adnexal MALT

Definitive

EBRT & electron beam

30 Gy in 15 fractions

5-year OS and local PFS were 100%

3-year disease PFS 100%

5-year disease PFS 93.3%

Acute: faint erythema, dry desquamation

Late: cataract(25%)

13

Desai et al., 2017

Ocular adnexal MALT

Definitive

EBRT

Electron & photon beam combination

22 to 45 Gy total dose

36 Gy in 20 fractions

30.6 Gy in 17 fractions

84.5% CR

Median OS was 250 months

Median PFS was 134 months

3.4% local relapse

No adverse event reported

14

Woolf et al., 2015

Ocular adnexal lymphoma

Definitive

EBRT & lens sparing technique

30-35 Gy in 15-20 fractions

OS 100%, 5% relapses

Acute: conjunctivitis, erythema, dry eye, photophobia, watery eye

Late: cataract, diplopia

15

Harada et al., 2014

Ocular adnexal MALT

Definitive

EBRT

Electron beam

30 Gy (3046 Gy in 2 Gy per fraction)

5-year OS 97.6%

10-year OS 93.5%

5-year LRFS: 98.7%

10-year LRFS: 98.7%

5-year CRFS: 97.0%

10-year CRFS: 90.8%

Cataracts developed in 20% eyes treated without lens shielding

16

Fasola et al., 2013

NHL of the ocular adnexa

Definitive & palliative

Electron beams & EBRT

4 Gy in 2 fractions over 2 consecutive days

CR: 85%

PR: 11%

SD: 4%

Mild acute side effects including dry eye, conjunctivitis, and transient periorbital edema

17

Hashimoto et al., 2012

Ocular adnexal MALT

Definitive

EBRT

Electron beam

3650 Gy/1825 fractions : 17 patients

3032.4 Gy/1518 fractions : 61 patients

5-year & 10-year OS: 98.1% and 95.3%

5-year RFS: 88.5%

10-year RFS: 75.9%

No local recurrence developed

10 patients relapsed distant tumors

Acute : mild conjunctivitis, dry eye, periorbital erythema/edema

Late : cataract, dry eye, glaucoma

Case reports

1

Meng et al., 2021

Ocular adnexal MALT

Definitive

EBRT

4 Gy in 2 fractions over 2 days

2 months after RT: reduced tumor mass

4 months after RT: complete resolution of diplopia

No adverse events reported

2

Saria et al., 2020

Conjunctival MALT lymphoma

Definitive

Brachytherapy

14 Gy at 23 mm depth

Complete resolution of the lesion

No adverse events reported

3

Ahluwalia et al., 2020

Ocular adnexal MALT

Definitive

EBRT

25.2 Gy to the inferior fornix

29.2 Gy to nasal palpebral conjunctiva

Complete resolution of the lesion

No adverse events reported

4

Cetingul et al., 2020

Ocular adnexal EMZL

Definitive

Electron beam

36 Gy in 17 Fractions

Rapid remission of the tumor

Acute erythema

5

Bennet, 2019

Conjunctival lymphoma

Definitive

EBRT

25 Gy in 10 fractions

Tumor regression at 4 months after RT

Cataract on the left eye, 4 years after RT

6

Cham and Riad, 2016

Ocular adnexal MALT

Definitive

EBRT

17 Gy in 15 fractions

CR and no progression

Dry eye

7

İncesoy-Özdemir et al., 2014

Ocular adnexal MALT

Definitive

EBRT

36 Gy

No local or systemic recurrences after 4 years

No adverse event reported

8

Palavi and Popescu-Martinez, 2014

Ocular adnexal lymphoma

Definitive

EBRT

30.6 Gy with fractions of 18 Gy/day

CR in 2 months

Remain tumor free at 8-month follow-up

No adverse event reported

Purpose and RT methods

The purpose of the studies was mostly either definitive or curative for as many as twenty-four studies (96%), and one study (4%) has both a curative and palliative intent. In terms of palliative treatment, RT was used to control the symptoms in non-localized disease. In terms of radiation source, almost all of the studies used external radiation and just three cases, reported by Saria et al., 2020, used internal radiation also known as brachytherapy. Besides, several planning methods were used, such as conventional or IMRT. Unfortunately, not all the studies mentioned their planning method nor use of lens shielding.

The total doses that were given to the tumor bed ranged from 4 Gy to 55 Gy. It can be categorized into three major groups, which are high dose, standard dose, and ultra-low dose. Patients who received 4–6 Gy were considered ultra-low dose RT, those who received 24–30.6 Gy were considered standard-dose RT, and those who received > 30.6 Gy were considered high-dose RT. The dose received is also determined by the location of the tumor. Because the radiation regimen could be considerably divided according to the primary site of OAML: whether it is the orbit, lacrimal gland, and lacrimal sac, known as orbital-type lymphoma, or the conjunctiva. Higher energy was used in the orbital-type lymphoma compared to the OAML in the conjunctiva.

Results

Between 75% and 90% patients showed complete response after receiving a full dose of radiation therapy. While 11–25% patients resulted in partial response. In addition, four out of eight case reports stated that their patient achieved partial response and remained tumor-free until the end of the follow up. Local relapse only reported by Desai et al. 2017 and Woolf et al. 2015 at 3.5% and 5% consecutively. Higher 5-year PFS was reported by Kim et al. 2020 in the patients group with lens shielding (90.1%) than the group without lens shielding (82.1%).

Kim et al., 2020 also reported an increase in Meiboscore after RT courses. The ratio of the meibomian gland area to the overall analyzed area dropped as the meiboscore grew. It may contribute to the occurrence of side effects. Dry eye was one of the common side effects from RT. Artificial tears were used to alleviate the symptoms, which subsided gradually over a few months. Other acute toxicities reported were periorbital soft tissue swelling, conjunctivitis, tearing/watery eye, and photophobia. The late toxicities that were commonly reported are cataract, xerophthalmia, retinal problem, and nasolacrimal duct obstruction. Xu et al. reported the median cataract incidence period was longer in the lens shielding group. Dry eye and cataract were the most common long-term side effects. IMRT patients had less grade 2 late toxicities (9%) than those treated with conventional procedures (33%), according to Rehn et al., 2020. When compared to standard-dose and high-dose RT, grade 1 late adverse effects (59% and 65% vs. 33%) and grade 2 late toxicities (6% and 31% vs. 0%) were less common after ultralow-dose RT.

Discussion

It is crucial to distinguish between intraocular lymphoma and orbital lymphoma since treatment and presentation are different. The most common sites for primary intraocular lymphoma are the retina or the uvea. Primary CNS lymphoma (PCNSL) is the most common type of the lymphoma in the retina, while the most common type of uveal primary lymphoma is the extranodal marginal zone also known as mucosa-associated lymphoid tissue (MALT) lymphoma. Intraocular lymphomas are usually localized in the eye, whereas orbital lymphomas do not affect intraocular tissue.

Orbital lymphoma or ocular adnexal lymphoma (OAL) is classified as primary if it affects only the ocular adnexa, and secondary if it is accompanied by another lymphoma of the same type. OAL is also classified by its location. It is classified as solitary if it just affects one or both orbits, extension if it affects nearby areas such as the sinuses, and systemic if it affects distant locations. About 55% of primary orbital tumors in adults were non-Hodgkin’s lymphoma. Most of the non-Hodgkin’s lymphoma of the orbit and adnexa are extranodal marginal zone B-cell lymphomas of mucosa-associated lymphoid tissue (EMZL of MALT) type or usually called ocular adnexal MALT lymphoma (OAML). Most cases present in patients between the ages of 15 and 70 years, but it strikes around the seventh decade of life [2, 3, 7].

Orbital lymphoma is the most common orbital lymphoproliferative lesion, which involves a wide range of conditions, from reactive lymphoid hyperplasia to lymphomas. The lacrimal sac, orbital soft tissue, extraocular muscles, lacrimal glands, eyelids, and conjunctiva can all be affected separately or in combination by these lesions [8]. In this review we focus on the OAML. The time it takes to diagnose OAML is undoubtedly influenced by the gradual and varied evolution of clinical symptoms, which are reliant on the anatomic sites where lymphomatous tissue is present. The unique “salmon red patch” appearance is caused by conjunctival involvement, which occurs in roughly 25% of all cases. A pink conjunctival mass or conjunctival hyperemia is the most common symptom. The other 75% of the cases have an intraorbital mass. Orbital lymphoma usually presents with mass-effect symptoms such as exophthalmos, ptosis, epiphora, ophthalmoplegia, and metamorphopsia [1, 9–10]. OAML is indicated by an indolent course and most are localized tumors which are preferred and mostly sensitive to radiotherapy (RT) [8].

RT was known to be an effective therapy as the initial treatment in orbital lymphoma. Orbital lymphoma with radiotherapy shows better local control and cure than surgery. RT is the treatment of choice for solitary low-grade lymphomas [11]. Several studies that used RT as a primary treatment for stage IE orbital lymphoma, were given 25–35 Gy to the tumor bed [12–16]. Although RT has been shown to provide excellent local control in cases of OAML, a few studies showed that ophthalmologic outcomes may be unfavorable because decreased visual acuity and deterioration of lens opacity occur in a dose-dependent way after radiation[17]. Therefore, in 2013, a study reported that low-dose radiation (2 × 2 Gy) in the treatment of orbital lymphoma is effective and well tolerated, with high response rates, durable local control, and minimal side effects [18]. This finding sparked other studies to assess the effectiveness of low-dose radiation in orbital lymphoma.

As more and more studies appear with different doses of radiotherapy, Rehn et al. conducted a study to compare three dose groups. Patients receiving 4–6 Gy were categorized as receiving ultra-low dose RT, 24–30.6 Gy as standard-dose RT, while those receiving > 30.6 Gy were categorized as receiving high-dose RT [19]. Different radiation doses and volumes had no significant effect on progression-free or overall survival, according to the study. In comparison to standard-dose and high-dose RT, ultra-low-dose RT was associated with a significantly lower rate of late toxicities. In addition, IMRT patients had significantly fewer acute toxicities and a trend toward lower late toxicities, compared to 3D-CRT or electrons patients. Three cases of conjunctival MALT of the fornix were treated with a focused single dose of 14 Gy kilovoltage brachytherapy that prescribed to the maximum thickness of the lesion, and after 40 months of follow-up, none of the three patients treated had any acute or chronic toxicities and were disease-free locally and distantly [20].

Radiation caused minimal acute adverse effects such as dry eye, conjunctivitis, and momentary periorbital edema. Artificial tears were usually effective in alleviating the symptoms. Cataract is the most commonly reported late effect of radiotherapy [19, 21–25]. Individuals who had lens protection had a lower 5-year risk of cataract formation than patients who did not have lens protection[21,22]. Patients who got30 Gy had a higher rate of cataract formation. There was no statistically significant link between underlying cataract risk factors such diabetes, hypertension, and contralateral cataract formation and symptomatic cataract formation [21].

Conclusion

RT is effective for treating low grade orbital MALT lymphoma as a primary definitive therapy with high survival rate, low recurrence rate, and generally acceptable toxicities. Until now, IMRT would be a better candidate for RT planning method because it provides lower toxicity. Different radiation doses and volumes have no significant effect on progression-free survival. However, ultra-low doses may result in a decreased rate of late toxicity.

Conflict of interest

The Authors declare that there is no conflict of interest.

Funding

This research received no specific grant from any funding agency in the public, commercial, or non-profit sectors.

Ethical permission

Ethical approval was not necessary for the preparation of this article.

Authors contribution

All authors contributed equally to this work.

Acknowledgement

We thank the following individuals for their expertise and assistance in all aspects of our study and for their help in writing the manuscript; also to all the authors whose articles we included in this study.

References

  1. Freedman K, Shenoy S. Mucosa-associated lymphoid tissue lymphoma with intraocular and orbital involvement: case presentation and review of the literature. Orbit. 2018; 37(4): 243–247, doi: 10.1080/01676830.2017.1383479, indexed in Pubmed: 29027822.
  2. Eckardt AM, Lemound J, Rana M, et al. Orbital lymphoma: diagnostic approach and treatment outcome. World J Surg Oncol. 2013; 11: 73, doi: 10.1186/1477-7819-11-73, indexed in Pubmed: 23506357.
  3. Desai A, Joag MG, Lekakis L, et al. Long-term course of patients with primary ocular adnexal MALT lymphoma: a large single-institution cohort study. Blood. 2017; 129(3): 324–332, doi: 10.1182/blood-2016-05-714584, indexed in Pubmed: 27789481.
  4. Platt S, Al Zahrani Y, Singh N, et al. Extranodal Marginal Zone Lymphoma of Ocular Adnexa: Outcomes following Radiation Therapy. Ocul Oncol Pathol. 2017; 3(3): 181–187, doi: 10.1159/000453615, indexed in Pubmed: 29134184.
  5. Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol. 2010; 25(9): 603–605, doi: 10.1007/s10654-010-9491-z, indexed in Pubmed: 20652370.
  6. Edwards JM, Shah PH, Huhn JL, et al. Definitive GRID and Fractionated Radiation in Bulky Head and Neck Cancer Associated With Low Rates of Distant Metastasis. Int J Radiat Oncol Biol Phys. 2015; 93(3): E334, doi: 10.1016/j.ijrobp.2015.07.1399.
  7. Lee J, Oh D, Choi BO, et al. Patterns of care for orbital marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue in Korea throughout 2016: Results from a multicenter cross-sectional cohort study (KROG 16-19). Asia Pac J Clin Oncol. 2019; 15(6): 358–363, doi: 10.1111/ajco.13221, indexed in Pubmed: 31264373.
  8. Rao R, Honavar SG. Orbital Tumors. In: Honavar SG. ed. Ocular Tumors. Springer, Singapore 155: 173.
  9. Woolf DK, Ahmed M, Plowman PN. Primary lymphoma of the ocular adnexa (orbital lymphoma) and primary intraocular lymphoma. Clin Oncol (R Coll Radiol). 2012; 24(5): 339–344, doi: 10.1016/j.clon.2012.03.001, indexed in Pubmed: 22521959.
  10. Annibali O, Sabatino F, Mantelli F, et al. Review article: Mucosa-associated lymphoid tissue (MALT)-type lymphoma of ocular adnexa. Biology and treatment. Crit Rev Oncol Hematol. 2016; 100: 37–45, doi: 10.1016/j.critrevonc.2016.01.009, indexed in Pubmed: 26857986.
  11. Olsen TG, Heegaard S. Orbital lymphoma. Surv Ophthalmol. 2019; 64(1): 45–66, doi: 10.1016/j.survophthal.2018.08.002, indexed in Pubmed: 30144455.
  12. Gveroviæ-Antunica A, Markoviæ I, Bohaè M, et al. Primary orbital non-Hodgkin’s lymphoma. Case report. Acta Clin Croat. 2007; 46: 113–116.
  13. De Cicco L, Cella L, Liuzzi R, et al. Radiation therapy in primary orbital lymphoma: a single institution retrospective analysis. Radiat Oncol. 2009; 4: 60, doi: 10.1186/1748-717X-4-60, indexed in Pubmed: 19968864.
  14. Kiesewetter B, Lukas J, Kuchar A, et al. Clinical features, treatment and outcome of mucosa-associated lymphoid tissue (MALT) lymphoma of the ocular adnexa: single center experience of 60 patients. PLoS One. 2014; 9(7): e104004, doi: 10.1371/journal.pone.0104004, indexed in Pubmed: 25077481.
  15. Rasmussen PK, Ralfkiaer E, Prause JU, et al. Follicular lymphoma of the ocular adnexal region: a nation-based study. Acta Ophthalmol. 2015; 93(2): 184–191, doi: 10.1111/aos.12525, indexed in Pubmed: 25125069.
  16. Cohen VM. Treatment options for ocular adnexal lymphoma (OAL). Clin Ophthalmol. 2009; 3: 689–692, doi: 10.2147/opth.s5828, indexed in Pubmed: 20054418.
  17. Kiesewetter B, Lukas J, Kuchar A, et al. Clinical features, treatment and outcome of mucosa-associated lymphoid tissue (MALT) lymphoma of the ocular adnexa: single center experience of 60 patients. PLoS One. 2014; 9(7): e104004, doi: 10.1371/journal.pone.0104004, indexed in Pubmed: 25077481.
  18. Fasola CE, Jones JC, Huang DD, et al. Low-dose radiation therapy (2 Gy × 2) in the treatment of orbital lymphoma. Int J Radiat Oncol Biol Phys. 2013; 86(5): 930–935, doi: 10.1016/j.ijrobp.2013.04.035, indexed in Pubmed: 23726002.
  19. Rehn S, Elsayad K, Oertel M, et al. Radiotherapy Dose and Volume De-escalation in Ocular Adnexal Lymphoma. Anticancer Res. 2020; 40(7): 4041–4046, doi: 10.21873/anticanres.14400, indexed in Pubmed: 32620650.
  20. Sarria GR, Cabrera CM, Sarria GJ, et al. Single-fraction low-energy electronic brachytherapy for conjunctival lymphoma. J Contemp Brachytherapy. 2020; 12(3): 267–272, doi: 10.5114/jcb.2020.96869, indexed in Pubmed: 32695199.
  21. Park HH, Lee SW, Sung SY, et al. Treatment outcome and risk analysis for cataract after radiotherapy of localized ocular adnexal mucosa-associated lymphoid tissue (MALT) lymphoma. Radiat Oncol J. 2017; 35(3): 249–256, doi: 10.3857/roj.2017.00374, indexed in Pubmed: 29037024.
  22. Xu L, Tang X, Jiang N, et al. Radiation Therapy Efficacy and Toxicity for Orbital and Ocular Adnexal Mucosa-Associated Lymphoid Tissue (OAMALT): A Single-Center, Retrospective Study of 32 Cases. Cancer Manag Res. 2021; 13: 8017–8024, doi: 10.2147/CMAR.S334396, indexed in Pubmed: 34707410.
  23. Platt S, Al Zahrani Y, Singh N, et al. Extranodal Marginal Zone Lymphoma of Ocular Adnexa: Outcomes following Radiation Therapy. Ocul Oncol Pathol. 2017; 3(3): 181–187, doi: 10.1159/000453615, indexed in Pubmed: 29134184.
  24. Shirota N, Nakayama H, Shiraishi S, et al. Target volume dose and clinical outcome in radiotherapy for primary marginal zone lymphoma of the ocular adnexa. Mol Clin Oncol. 2017; 6(6): 833–838, doi: 10.3892/mco.2017.1241, indexed in Pubmed: 28588773.
  25. Hashimoto N, Sasaki R, Nishimura H, et al. Long-term outcome and patterns of failure in primary ocular adnexal mucosa-associated lymphoid tissue lymphoma treated with radiotherapy. Int J Radiat Oncol Biol Phys. 2012; 82(4): 1509–1514, doi: 10.1016/j.ijrobp.2011.04.052, indexed in Pubmed: 21664061.
  26. Lee MJ, Lee MeY, Choe JY, et al. Ultra-low-dose radiation treatment for early-stage ocular adnexal MALT lymphoma. Eur J Ophthalmol. 2021 [Epub ahead of print]: 11206721211035622, doi: 10.1177/11206721211035622, indexed in Pubmed: 34318737.
  27. Leeson S, Jayamohan J, Vu H, et al. Examining the utility of lower dose radiotherapy for localised primary ocular adnexal MALT lymphoma. J Med Radiat Sci. 2021; 68(3): 269–273, doi: 10.1002/jmrs.464, indexed in Pubmed: 33675287.
  28. Niwa M, Ishikura S, Tatekawa K, et al. Radiotherapy alone for stage IE ocular adnexal mucosa-associated lymphoid tissue lymphomas: long-term results. Radiat Oncol. 2020; 15(1): 25, doi: 10.1186/s13014-020-1477-8, indexed in Pubmed: 32000814.
  29. Kim SE, Yang HJ, Yang SW. Effects of radiation therapy on the meibomian glands and dry eye in patients with ocular adnexal mucosa-associated lymphoid tissue lymphoma. BMC Ophthalmol. 2020; 20(1): 24, doi: 10.1186/s12886-019-1301-0, indexed in Pubmed: 31931766.
  30. Jeon YW, Yang HJ, Choi BO, et al. Comparison of Selection and Long-term Clinical Outcomes Between Chemotherapy and Radiotherapy as Primary Therapeutic Modality for Ocular Adnexal MALT Lymphoma. EClinicalMedicine. 2018; 4-5: 32–42, doi: 10.1016/j.eclinm.2018.10.001, indexed in Pubmed: 31193655.
  31. Pinnix CC, Dabaja BS, Milgrom SA, et al. Ultra-low-dose radiotherapy for definitive management of ocular adnexal B-cell lymphoma. Head Neck. 2017; 39(6): 1095–1100, doi: 10.1002/hed.24717, indexed in Pubmed: 28370694.
  32. Li Y, Wu FT, Wang Li, et al. Ocular adnexal mucosa-associated lymphoid tissue lymphoma: a single center experience of 32 patients from China. Int J Clin Exp Pathol. 2018; 11(3): 1520–1528, indexed in Pubmed: 31938249.
  33. Woolf DK, Kuhan H, Shoffren O, et al. Outcomes of primary lymphoma of the ocular adnexa (orbital lymphoma) treated with radiotherapy. Clin Oncol (R Coll Radiol). 2015; 27(3): 153–159, doi: 10.1016/j.clon.2014.10.002, indexed in Pubmed: 25455843.
  34. Harada K, Murakami N, Kitaguchi M, et al. Localized ocular adnexal mucosa-associated lymphoid tissue lymphoma treated with radiation therapy: a long-term outcome in 86 patients with 104 treated eyes. Int J Radiat Oncol Biol Phys. 2014; 88(3): 650–654, doi: 10.1016/j.ijrobp.2013.11.235, indexed in Pubmed: 24521680.
  35. Meng K, Lim MC, Poon ML, et al. Low-dose ‘boom-boom’ radiotherapy for ocular lymphoma arising from IgG4-related ophthalmic disease: Case report and literature review. Eur J Ophthalmol. 2021 [Epub ahead of print]: 11206721211018372, doi: 10.1177/11206721211018372, indexed in Pubmed: 34030509.
  36. Ahluwalia A, Feng PW, Meskin SW. Ocular adnexal lymphoma presenting as incidental tarsal follicles. Am J Ophthalmol Case Rep. 2020; 19: 100731, doi: 10.1016/j.ajoc.2020.100731, indexed in Pubmed: 32426554.
  37. Çetingül N, Palamar M, Hacıkara Ş, et al. Extranodal Ocular Adnexal Marginal Zone Lymphoma in a Ten-Year-Old Child. Turk J Ophthalmol. 2020; 50(1): 53–55, doi: 10.4274/tjo.galenos.2019.62592, indexed in Pubmed: 32167265.
  38. Bennett LW. Case Report: Primary Conjunctival Non-Hodgkin Marginal Zone Lymphoma. Optom Vis Sci. 2019; 96(2): 133–136, doi: 10.1097/OPX.0000000000001337, indexed in Pubmed: 30589762.
  39. Cham KM, Riad H. Salmon-coloured lesions mimicking conjunctival papillae: an unusual presentation of unilateral conjunctival lymphoma in a young man. Clin Exp Optom. 2016; 99(3): 289–292, doi: 10.1111/cxo.12400, indexed in Pubmed: 27121644.
  40. İncesoy-Özdemir S, Yüksek N, Bozkurt C, et al. A rare type of cancer in children: extranodal marginal zone B-cell (MALT) lymphoma of the ocular adnexa. Turk J Pediatr. 2014; 56(3): 295–298, indexed in Pubmed: 25341603.
  41. Pallavi R, Popescu-Martinez A. More than meets the eye: the ‘pink salmon patch’. BMJ Case Rep. 2014; 2014, doi: 10.1136/bcr-2014-204357, indexed in Pubmed: 25168823.
  42. Astafurov KV, Bothun ED, Laack NN, et al. Ultra-low-dose (boom-boom) radiotherapy for management of recurrent ocular post-transplant lymphoproliferative disorder. Am J Ophthalmol Case Rep. 2021; 23: 101118, doi: 10.1016/j.ajoc.2021.101118, indexed in Pubmed: 34041417.



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